The search resulted in 55 diseases.
Orphanet:1260 Sino-auricular heart block
Orphanet:1344 Atrial standstill
Orphanet:1369 Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome
Orphanet:154 Familial isolated dilated cardiomyopathy
Orphanet:217085 Mucopolysaccharidosis type 2, severe form
Orphanet:228012 Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome
Orphanet:26791 Multiple acyl-CoA dehydrogenase deficiency
Orphanet:273 Steinert myotonic dystrophy
Orphanet:319646 PGM1-CDG
Orphanet:324 Fabry disease
Orphanet:324525 Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation
Orphanet:3282 Multifocal atrial tachycardia
Orphanet:329874 Idiopathic giant cell myocarditis
Orphanet:3403 Uhl anomaly
Orphanet:34217 Naxos disease
Orphanet:550 MELAS
Orphanet:551 MERRF
Orphanet:563 Peripartum cardiomyopathy
Orphanet:580 Mucopolysaccharidosis type 2
Orphanet:59306 McLeod neuroacanthocytosis syndrome
Orphanet:66529 Tako-Tsubo cardiomyopathy
Orphanet:75249 Familial isolated restrictive cardiomyopathy
Orphanet:77259 Gaucher disease type 1
Orphanet:77260 Gaucher disease type 2
Orphanet:77261 Gaucher disease type 3
Orphanet:797 Sarcoidosis
Orphanet:844 Atrial tachyarrhythmia with short PR interval
Orphanet:871 Familial progressive cardiac conduction defect
Orphanet:93473 Hurler syndrome
Orphanet:93567 Pediatric systemic sclerosis
OMIM:115197 Cardiomyopathy, familial hypertrophic, 4
OMIM:115210 Cardiomyopathy, familial restrictive, 1
OMIM:192600 Cardiomyopathy, familial hypertrophic, 1
OMIM:601494 Cardiomyopathy, dilated, 1D
OMIM:604401 Arrhythmogenic right ventricular dysplasia, familial, 6
OMIM:607482 Cardiomyopathy, dilated, 1M
OMIM:607487 Cardiomyopathy, hypertrophic, 25
OMIM:610193 Arrhythmogenic right ventricular dysplasia, familial, 10
OMIM:611407 Cardiomyopathy, dilated, 1W
OMIM:611615 Cardiomyopathy, dilated, 1X
OMIM:611878 Cardiomyopathy, dilated, 1Y
OMIM:611879 Cardiomyopathy, dilated, 1Z
OMIM:611880 Cardiomyopathy, dilated, 2A
OMIM:612124 Cardiomyopathy, familial hypertrophic, 12
OMIM:612877 Cardiomyopathy, dilated, 1BB
OMIM:613243 Cardiomyopathy, familial hypertrophic, 13
OMIM:613251 Cardiomyopathy, familial hypertrophic, 14
OMIM:613690 Cardiomyopathy, familial hypertrophic, 7
OMIM:613838 Cardiomyopathy, familial hypertrophic, 16
OMIM:613873 Cardiomyopathy, familial hypertrophic, 17
OMIM:615396 Left ventricular noncompaction 10
Orphanet:420429 Glycogen storage disease due to acid maltase deficiency, late-onset
Orphanet:436242 Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease
OMIM:609578 Cardiomyopathy, familial restrictive 2
OMIM:609915 Cardiomyopathy, dilated, 1Q